ClinVar Miner

Submissions for variant NM_138413.4(HOGA1):c.835-7T>A

dbSNP: rs768061627
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002537790 SCV003349947 likely benign not provided 2022-04-30 criteria provided, single submitter clinical testing
Natera, Inc. RCV001278338 SCV001465340 uncertain significance Primary hyperoxaluria type 3 2020-04-11 no assertion criteria provided clinical testing

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